美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA208717"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
72241-035-04 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (72241-035-04)
72241-035-05 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (72241-035-05)
72241-035-11 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 1000 TABLET in 1 BOTTLE (72241-035-11)
72241-035-22 72241-035 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (72241-035-22)
71209-058-01 71209-058 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 30 TABLET in 1 BOTTLE (71209-058-01)
71209-058-04 71209-058 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (71209-058-04)
71209-058-05 71209-058 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (71209-058-05)
71209-058-11 71209-058 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 1000 TABLET in 1 BOTTLE (71209-058-11)
72162-2414-3 72162-2414 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20241031 N/A ANDA ANDA208717 Bryant Ranch Prepack NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (72162-2414-3)
72162-2414-9 72162-2414 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20241031 N/A ANDA ANDA208717 Bryant Ranch Prepack NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (72162-2414-9)
72241-034-04 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (72241-034-04)
72241-034-05 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (72241-034-05)
72241-034-11 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (72241-034-11)
72241-034-22 72241-034 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (72241-034-22)
71209-061-01 71209-061 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 30 TABLET in 1 BOTTLE (71209-061-01)
71209-061-04 71209-061 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 90 TABLET in 1 BOTTLE (71209-061-04)
71209-061-05 71209-061 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 100 TABLET in 1 BOTTLE (71209-061-05)
71209-061-11 71209-061 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20181016 N/A ANDA ANDA208717 Cadila Pharmaceuticals Limited NEBIVOLOL HYDROCHLORIDE 20 mg/1 1000 TABLET in 1 BOTTLE (71209-061-11)
72241-032-04 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 90 TABLET in 1 BOTTLE (72241-032-04)
72241-032-05 72241-032 HUMAN PRESCRIPTION DRUG Nebivolol Nebivolol TABLET ORAL 20211218 N/A ANDA ANDA208717 Modavar Pharmaceuticals LLC NEBIVOLOL HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (72241-032-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase